Quality Lab Senior Supervisor
Job Category: Quality Management / Pharmaceutical / Laboratory
Reference ID: JR-182297
Location: Marion, North Carolina, United States
Company: Baxter International Inc.
Employment Type: Full-Time
Work Authorization: U.S. work authorization required (no visa sponsorship available)
About the Organization
Baxter International Inc. is a global leader in pharmaceutical and medical device manufacturing. The company is dedicated to improving patient safety and outcomes through high-quality products, regulatory compliance, and operational excellence. Baxter’s culture emphasizes collaboration, integrity, and continuous innovation, providing employees with opportunities to make a tangible impact on global healthcare.
Position Overview
The Quality Lab Senior Supervisor will oversee the QC Particulate Matter Laboratory operations, ensuring compliance with regulatory standards, company SOPs, and cGMP guidelines. This role combines leadership, technical expertise, and operational management to maintain high-quality laboratory outcomes and drive continuous improvement.
The ideal candidate will have extensive experience in pharmaceutical or medical device laboratory environments, strong supervisory skills, and a proven ability to manage laboratory teams effectively.
Key Responsibilities
Lead and manage all activities for the assigned QC Particulate Matter Laboratory shift.
Supervise, mentor, and develop laboratory personnel, including conducting performance reviews, training, and ACE check-ins.
Coordinate testing in accordance with USP <1790> and USP <788> methodologies, ensuring accuracy, efficiency, and compliance.
Oversee data recording, review, and analysis; address documentation errors and ensure timely submission for release.
Troubleshoot laboratory and equipment issues, providing guidance and support for staff as needed.
Conduct investigations for non-conformance, deviations, and quality incidents using TrackWise 8.
Ensure adherence to aseptic techniques, microbiological testing standards, and laboratory safety protocols.
Participate in cross-training within the QC Microbiology Laboratory to support operational flexibility and knowledge sharing.
Collaborate with Quality Management to implement continuous improvement initiatives and resolve quality challenges.
Required Qualifications & Experience
Bachelor’s degree in a Life Science field (Biology, Microbiology, or related).
Minimum 5 years of laboratory experience in a pharmaceutical or medical device setting, with supervisory experience preferred.
Master’s degree in biological sciences with applied laboratory experience is advantageous.
In-depth knowledge of aseptic techniques, microbiological testing, and compliance with FDA, cGMP, GLP, and USP standards.
Proficient with Microsoft Office applications (Word, Excel) and quality management systems (TrackWise 8).
Strong organizational, multitasking, and problem-solving skills.
Ability to foster a positive, collaborative work environment and develop team members effectively.
Willingness to work in laboratory and manufacturing environments while adhering to PPE requirements.
Compensation & Benefits
Estimated base salary: $88,000 – $121,000 annually, with eligibility for discretionary bonuses.
Comprehensive health coverage including medical, dental, and vision from day one.
Paid Time Off (160 hours) and paid holidays.
401(k) Retirement Savings Plan with company match and Employee Stock Purchase Program (ESPP).
Tuition reimbursement and paid parental leave.
Shift flexibility and overtime opportunities.
Additional benefits include wellness programs, commuting support, employee discounts, and childcare assistance.
Equal Employment Opportunity
Baxter International Inc. is an equal opportunity employer. All qualified applicants will be considered without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity, veteran status, disability, or any other legally protected characteristic.
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